Engilbert Sigurðsson
Impact in
- Biological Psychiatry top 0.05%
- Tryptophan and brain disorders
- Genetics top 0.05%
- Genetic Associations and Epidemiology
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
Papers in
- Genetics 72
- Genetic Associations and Epidemiology 45
- Genetics and Neurodevelopmental Disorders 19
- Genomic variations and chromosomal abnormalities 17
- Genomics and Rare Diseases 17
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- Schizophrenia research and treatment 15
- Bipolar Disorder and Treatment 11
- Attention Deficit Hyperactivity Disorder 6
- Co-authors
- Eric J Fombonne (3 shared papers)Jim van Os (2 shared papers)Brynja Björk Magnúsdóttir (14 shared papers)Kapil S. Sayal (1 shared paper)Stuart A. Checkley (1 shared paper)James Hunter MacCabe (5 shared papers)Magnus H. Haraldsson (8 shared papers)Hannes Pétursson (8 shared papers)
- Journals
- Molecular Psychiatry (11 papers)Biological Psychiatry (10 papers)Nature Genetics (9 papers)Nature (7 papers)The American Journal of Human Genetics (6 papers)
- Partner nations
- IcelandUnited KingdomUnited States
In The Last Decade
Engilbert Sigurðsson
135 papers receiving 28.9k citations
Engilbert Sigurðsson's Hit Papers
Peers
Comparison fields: 5 of 180
- Biological Psychiatry 2.6k
- Genetics 13.9k
- Psychiatry and Mental health 4.3k
- Behavioral Neuroscience 765
- Cognitive Neuroscience 3.4k
Countries citing papers authored by Engilbert Sigurðsson
This map shows the geographic impact of Engilbert Sigurðsson's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Engilbert Sigurðsson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Engilbert Sigurðsson more than expected).
Fields of papers citing papers by Engilbert Sigurðsson
This network shows the impact of papers produced by Engilbert Sigurðsson. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Engilbert Sigurðsson. The network helps show where Engilbert Sigurðsson may publish in the future.
Co-authors
The 25 scholars most cited alongside Engilbert Sigurðsson, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 142 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Biological insights from 108 schizophrenia-associated genetic loci Hit paper breakdown → | 2014 | 6062 |
| 2 | Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression Hit paper breakdown → | 2018 | 2171 |
| 3 | Genome-wide association study identifies five new schizophrenia loci Hit paper breakdown → | 2011 | 1643 |
| 4 | Mapping genomic loci implicates genes and synaptic biology in schizophrenia Hit paper breakdown → | 2022 | 1614 |
| 5 | Large recurrent microdeletions associated with schizophrenia Hit paper breakdown → | 2008 | 1412 |
| 6 | Common variants conferring risk of schizophrenia Hit paper breakdown → | 2009 | 1402 |
| 7 | Neuregulin 1 and Susceptibility to Schizophrenia Hit paper breakdown → | 2002 | 1392 |
| 8 | Genome-wide association analysis identifies 13 new risk loci for schizophrenia Hit paper breakdown → | 2013 | 1231 |
| 9 | Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection Hit paper breakdown → | 2018 | 1079 |
| 10 | Genome-wide association study identifies 30 loci associated with bipolar disorder Hit paper breakdown → | 2019 | 1065 |
| 11 | Genomic Relationships, Novel Loci, and Pleiotropic Mechanisms across Eight Psychiatric Disorders Hit paper breakdown → | 2019 | 965 |
| 12 | Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology Hit paper breakdown → | 2021 | 938 |
| 13 | A mega-analysis of genome-wide association studies for major depressive disorder Hit paper breakdown → | 2012 | 931 |
| 14 | Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes Hit paper breakdown → | 2018 | 543 |
| 15 | CNVs conferring risk of autism or schizophrenia affect cognition in controls Hit paper breakdown → | 2013 | 540 |
| 16 | Partitioning Heritability of Regulatory and Cell-Type-Specific Variants across 11 Common Diseases Hit paper breakdown → | 2014 | 431 |
| 17 | 2008 | 390 | |
| 18 | 2011 | 372 | |
| 19 | 2015 | 294 | |
| 20 | 2011 | 236 |
About Engilbert Sigurðsson
Engilbert Sigurðsson is a scholar working on Genetics, Psychiatry and Mental health, Pediatrics, Perinatology and Child Health, Experimental and Cognitive Psychology and Clinical Psychology, having authored 142 papers that have together received 29.6k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (45 papers), Genetics and Neurodevelopmental Disorders (19 papers), Genomic variations and chromosomal abnormalities (17 papers), Genomics and Rare Diseases (17 papers), Schizophrenia research and treatment (15 papers), Bipolar Disorder and Treatment (11 papers), Epigenetics and DNA Methylation (9 papers) and Attention Deficit Hyperactivity Disorder (6 papers). The work is most often cited by research in Biological Psychiatry (2.6k citations), Genetics (13.9k citations), Psychiatry and Mental health (4.3k citations), Behavioral Neuroscience (765 citations) and Cognitive Neuroscience (3.4k citations). Engilbert Sigurðsson has collaborated with scholars based in Iceland, United Kingdom and United States. Frequent co-authors include Eric J Fombonne, Jim van Os, Brynja Björk Magnúsdóttir, Kapil S. Sayal, Stuart A. Checkley, James Hunter MacCabe, Magnus H. Haraldsson, Hannes Pétursson, Steinunn Bækkeskov and Helgi Sigvaldason. Their work appears in journals such as Molecular Psychiatry, Biological Psychiatry, Nature Genetics, Nature and The American Journal of Human Genetics.
Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.